HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557256Generated: October 25, 2026
N-methyl-2-pyrrolidone → HCID 131729277, compound
https://huagongshe.com/reaction/557256
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-3-iodopyridine | HCID 2763151 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131729277 | HCID 131729277 | — |
Reaction Steps
To a mixture of 3-iodo-pyridin-2-ylamine described in Preparation Example 1-1-3 (40.2 g, 183 mmol), trimethylsilyl acetylene (51.7 mL, 366 mmol), copper(I) iodide (3.49 g, 18.3 mmoL), N,N-diisopropyl ethyl amine (63.7 mL, 366 mmol), N-methylpyrrolidinone (200 mL) was added tetrakis(triphenyl phosphine) palladium (0) (10.6 g, 9.15 mmol), which was stirred at room temperature for 3 hours 10 minutes under a nitrogen stream. To the reaction solution was added water and extracted four times with ethyl acetate. The solvent thereof was concentrated under a reduced pressure. The residue was purified by NH silica gel chromatography (heptane:ethyl acetate=4:1). The resulting solution was concentrated under a reduced pressure and the residue was purified by silica gel chromatography (heptane:ethyl acetate=2:1 then 1:1) to obtain the title compound (28.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058444B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b26c6ec978b342c0a2020066a95e03ba |
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| Source note | uspto-grants-2011_11 |
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